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| Product | Description | |
|---|---|---|
| Ubenimex | 250mg Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C16H24N2O4. CAS No. 58970-76-6. Prepack ID 89989951-250mg. Molecular Weight 308.37. See USA prepack pricing. |  |
| Ubenimex | Ubenimex (INN), also known more commonly as bestatin, is a competitive, reversible protease inhibitor. It is an inhibitor of arginyl aminopeptidase (aminopeptidase B), leukotriene A4 hydrolase (a zinc metalloprotease that displays both epoxide hydrolase and aminopeptidase activities), alanyl aminopeptidase (aminopeptidase M/N), leucyl/cystinyl aminopeptidase (oxytocinase/vasopressinase), and membrane dipeptidase (leukotriene D4 hydrolase). It is being studied for use in the treatment of acute myelocytic leukemia. It is derived from Streptomyces olivoreticuli. Ubenimex has been found to inhibit the enzymatic degradation of oxytocin, vasopressin, enkephalins, and various other peptides and compounds. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3-(r)-amino-2-(s)-hydroxy-4-phenylbutanoyl-(s)-leucine;n-(3-amino-2-hydroxy-1-oxo-4-phenylbutyl)-,(s-(r*,s*))-l-leucin;nk421;UBENIMEX;N-[(2S,3R)-3-AMINO-2-HYDROXY-1-OXO-4-PHENYLBUTYL]-L-LEUCINE;N-((2S,3R)-3-AMINO-2-HYDROXY-4-PHENYLBUTYRYL)-L-LEUCINE;[(2S,3R)-3-AMINO-2-HYDROXY-4-PHENYLBUTYRYL]-L-LEUCINE;[(2S,3R)-3-AMINO-2-HYDROXY-4-PHENYLBUTANOYL]-LEU. Appearance: White crystalline powder. CAS No. 58970-76-6. Molecular formula: C16H24N2O4. Mole weight: 308.37. Purity: 0.99. IUPACName: (2S)-2-[[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanoyl]amino]-4-methylpentanoicacid. Canonical SMILES: CC(C)CC(C(=O)O)NC(=O)C(C(CC1=CC=CC=C1)N)O. Density: 1.197 g/ |  |
| Ubenimex USP | N-[(2S,3R)-3-Amino-2-hydroxy-4-phenylbutyryl]-L-leucine. anti-hypertensive. Grades: USP. CAS No. 58970-76-6. Product ID: 8-04676. Molecular formula: C16H24N2O4. Mole weight: 308.08. |  |
| UBE Polyethylene | UBE Polyethylene. Group: Polymers. |  |
| Ubidecarenone | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Ubiquinone 10, Li-Q-Sorb, Ubiquinone 50, Unispheres Q 10, (all-E)-2-(3,7,11,15,19,23,27,31,35,39-Decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl)-5,6-dimethoxy-3-methyl-2,5-cyclohexadiene-1,4-dione, Kudesan, p-Benzoquinone, 2-(3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl)-5,6-dimethoxy-3-methyl- (8CI), PureSorb Q 40, Q 10AA, Vitamin Q, Ensorb, Kaneka Q10, Q-Gel 100,Ubidecarenone, Q-absorb, NSC 140865, Q-Gel, 2,5-Cyclohexadiene-1,4-dione, 2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl]-5,6-dimethoxy-3-methyl- (9CI), Ubiquinone Q10, Liquid-Q, Neuquinon, Aqua Q 10L10, Bio-Quinone Q10, Adelir, 2,5-Cyclohexadiene-1,4-dione, 2-(3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl)-5,6-dimethoxy-3-methyl-, (all-E)-, Aqua Q10, Coenzyme Q10 (6CI), Ubiquinone, Q10, 2-[(all-E)-3,7,11,15,19,23,27,31,35,39-Decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-5,6-dimethoxy-3-methylbenzene-1,4-dione, CoQ10, Aqua-Q 10P40, Neuquinone, Cosmesome Q 10, Bio-Quinon, Cudesan. |  |
| Ubidecarenone for system suitability | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Kaneka Q10, Aqua Q 10L10, Ubiquinone Q10, Unispheres Q 10, (all-E)-2-(3,7,11,15,19,23,27,31,35,39-Decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl)-5,6-dimethoxy-3-methyl-2,5-cyclohexadiene-1,4-dione, Kudesan, Aqua Q10, PureSorb Q 40, Bio-Quinon, Cosmesome Q 10,Ubidecarenone, Li-Q-Sorb, Q-absorb, NSC 140865, CoQ10, Ubiquinone 50, Adelir, Ensorb, Q-Gel, Q-Gel 100, Neuquinone, Ubiquinone 10, 2,5-Cyclohexadiene-1,4-dione, 2-(3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl)-5,6-dimethoxy-3-methyl-, (all-E)-, 2,5-Cyclohexadiene-1,4-dione, 2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl]-5,6-dimethoxy-3-methyl- (9CI), Q10, Ubiquinone, Liquid-Q, Coenzyme Q10 (6CI), Q 10AA, Vitamin Q, Neuquinon, Bio-Quinone Q10, Cudesan, p-Benzoquinone, 2-(3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl)-5,6-dimethoxy-3-methyl- (8CI), 2-[(all-E)-3,7,11,15,19,23,27,31,35,39-Decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-5,6-dimethoxy-3-methylbenzene-1,4-dione, Aqua-Q 10P40. | |
| Ubidecarenone Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Ubiquicidin | Ubiquicidin is a synthetic cationic antimicrobial peptide. It has activity against gram-positive bacteria and gram-negative bacteria. Synonyms: Lys-Val-His-Gly-Ser-Leu-Ala-Arg-Ala-Gly-Lys-Val-Arg-Gly-Gln-Thr-Pro-Lys-Val-Ala-Lys-Gln-Glu-Lys-Lys-Lys-Lys-Lys-Thr-Gly-Arg-Ala-Lys-Arg-Arg-Met-Gln-Tyr-Asn-Arg-Arg-Phe-Val-Asn-Val-Val-Pro-Thr-Phe-Gly-Lys-Lys-Lys-Gly-Pro-Asn-Ala-Asn-Ser. Mole weight: 6648. |  |
| Ubiquinol | Ubiquinol. CAS No: 992-78-9 |  Sarchem Laboratories New Jersey NJ |
| Ubiquinol | Reduced coenzyme Q for improving nervous system cell functions. Group: Biochemicals. Alternative Names: 2-[(2E, 6E, 10E, 14E, 18E, 22E, 26E, 30E, 34E)-3, 7, 11, 15, 19, 23, 27, 31, 35, 39-Decamethyl-2, 6, 10, 14, 18, 22, 26, 30, 34, 38-tetracontadecaen-1-yl]-5, 6-dimethoxy-3-methyl- 1,4-benzenediol; Dihydrocoenzyme Q10; Reduced Coenzyme Q10; Reduced Ubiquinone Q10; Ubiquinol 50. Grades: Highly Purified. CAS No. 992-78-9. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Ubiquinol | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| ubiquinol oxidase (electrogenic, non H+-transporting) | This terminal oxidase enzyme is unable to pump protons but generates a proton motive force by transmembrane charge separation resulting from utilizing protons and electrons originating from opposite sides of the membrane to generate water. The bioenergetic efficiency (the number of charges driven across the membrane per electron used to reduce oxygen to water) is 1. The bd-I oxidase from the bacterium Escherichia coli is the predominant respiratory oxygen reductase that functions under microaerophilic conditions in that organism. cf. EC 1.10.3.10, ubiquinol oxidase (H+-transporting). Group: Enzymes. Synonyms: cytochrome bd-I oxidase; cydA (gene name); cydB (gene name); ubiquinol:O2 oxidoreductase (electrogenic, non H+-transporting). Enzyme Commission Number: EC 7.1.1.7 (Formerly EC 1.10.3.14). Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0480; ubiquinol oxidase (electrogenic, non H+-transporting); EC 1.10.3.14; cytochrome bd-I oxidase; cydA (gene name); cydB (gene name); ubiquinol:O2 oxidoreductase (electrogenic, non H+-transporting). Cat No: EXWM-0480. |  |
| ubiquinol oxidase (H+-transporting) | Contains a dinuclear centre comprising two hemes, or heme and copper. This terminal oxidase enzyme generates proton motive force by two mechanisms: (1) transmembrane charge separation resulting from utilizing protons and electrons originating from opposite sides of the membrane to generate water, and (2) active pumping of protons across the membrane. The bioenergetic efficiency (the number of charges driven across the membrane per electron used to reduce oxygen to water) depends on the enzyme; for example, for the bo3 oxidase it is 2, while for the bd-II oxidase it is 1. cf. EC 1.10.3.14, ubiquinol oxidase (electrogenic, non H+-transporting). Group: Enzymes. Synonyms: cytochrome bb3 oxidase; cytochrome bo oxidase; cytochrome bd-II oxidase; ubiquinol:O2 oxidoreductase (H+-transporting). Enzyme Commission Number: EC 7.1.1.3 (Formerly EC 1.10.3.10). Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0476; ubiquinol oxidase (H+-transporting); EC 1.10.3.10; cytochrome bb3 oxidase; cytochrome bo oxidase; cytochrome bd-II oxidase; ubiquinol:O2 oxidoreductase (H+-transporting). Cat No: EXWM-0476. | |
| ubiquinol oxidase (non-electrogenic) | The enzyme, described from the mitochondria of plants and some fungi and protists, is an alternative terminal oxidase that is not sensitive to cyanide inhibition and does not generate a proton motive force. Unlike the electrogenic terminal oxidases that contain hemes (cf. EC 1.10.3.10 and EC 1.10.3.14), this enzyme contains a dinuclear non-heme iron complex. The function of this oxidase is believed to be dissipating excess reducing power, minimizing oxidative stress, and optimizing photosynthesis in response to changing conditions. Group: Enzymes. Synonyms: plant alternative oxidase; cyanide-insensitive oxidase; AOX (gene name); ubiquinol oxidase; ubiquinol:O2 oxidoreductase (non-electrogenic). Enzyme Commission Number: EC 1.10.3.11. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0477; ubiquinol oxidase (non-electrogenic); EC 1.10.3.11; plant alternative oxidase; cyanide-insensitive oxidase; AOX (gene name); ubiquinol oxidase; ubiquinol:O2 oxidoreductase (non-electrogenic). Cat No: EXWM-0477. | |
| Ubiquinone-1 | Ubiquinone-1 is an intermediate in the synthesis of Coenzyme Q. Ubiquinone-1 can be reduced by NADPH oxidase, hepatoma cells, Ascorbic acid (HY-B0166)[1][2][3][4][5]. Uses: Scientific research. Group: Natural products. CAS No. 727-81-1. Pack Sizes: 1 mg (40 mM * 100 ?L in Ethanol); 5 mg (40 mM * 500 ?L in Ethanol); 10 mg (40 mM * 1 mL in Ethanol); 25 mg (40 mM * 2.5 mL in Ethanol); 50 mg (40 mM * 5 mL in Ethanol); 100 mg (40 mM * 10 mL in Ethanol). Product ID: HY-113449. |  |
| Ubiquinone-10 | Ubiquinone-10 acts as an inhibitor of the mitochondrial permeability transition pore (MPTP). This inhibitory effect can be counteracted by ubiquinone-5. Applications: An inhibitor of the mitochondrial permeability transition pore. Group: Coenzymes. Synonyms: Coenzyme Q2; 2,3-Dimethoxy-5-methyl-6-geranyl-1,4-benzoquinone. CAS No. 606-06-4. Purity: ≥90%. Mole weight: 318.4. Form: Liquid. Coenzyme Q2; 2,3-Dimethoxy-5-methyl-6-geranyl-1,4-benzoquinone; Ubiquinone-10; 606-06-4. Cat No: COEC-062. | |
| Ubiquinone-5 | Ubiquinone-5 is a coenzyme Q10 (CoQ10) (sc-205262) analog that counteracts the inhibitory effects on mitochondrial permeability transition pore (MPTP) of decylubiquinone and ubiquinone-10. Applications: A coq10 analog that counteracts the inhibitory effects on mptp. Group: Coenzymes. Synonyms: Coenzyme Q1. CAS No. 727-81-1. Mole weight: 250.29. Form: Liquid. Coenzyme Q1; Ubiquinone-5; 727-81-1. Cat No: COEC-012. | |
| Ubiquitin-13C,15N,D human | ?98 atom %, ?90% (CP), recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-13C,15N human | ?98 atom %, ?90% (CP), recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-15N,D human | 97 atom % D, 98 atom % 15N, recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-15N human | 98 atom % 15N, recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-7-amido-4-methylcoumarin | solution (supplied in DMSO). Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin Activating Enzyme (E1) human | recombinant, expressed in baculovirus infected Sf21 cells. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin?Agarose | saline suspension. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin Aldehyde | Potent and specific inhibitor of multiple ubiquitin hydrolases involved in pathways of intracellular protein modification and turnover. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin Aldehyde human | recombinant, expressed in E. coli, ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitination Compound Library | A unique collection of 214 ubiquitination related small chemicals can be used for high throughput and high content screening?- Targets include proteasome, E1/E2/E3 Enzyme, DUB, p97, etc. ; - Detailed compound information with structure, target, and biological activity description?- NMR and HPLC validated to ensure high purity and quality. Uses: Scientific use. Product Category: L8600. Categories: Ubiquitination Compounds Libraries. |  |
| Ubiquitin-Carrier Protein H10 human | ?95% (SDS-PAGE), recombinant, expressed in E. coli (histidine-tagged), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin Carrier Protein H3/CDC34 human | ?95% (SDS-PAGE), recombinant, expressed in E. coli overproducing strain. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-Carrier Protein H5a, GST-tagged human | ?95% (SDS-PAGE), liquid. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-Carrier Protein H5b human | ?95% (SDS-PAGE), solution. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-Carrier Protein H5c human | ?95% (SDS-PAGE), recombinant, expressed in E. coli (GST-tagged), solution. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-Carrier Protein H7 human | ?95% (SDS-PAGE), recombinant, expressed in E. coli, liquid. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin E1 Inhibitor, PYR-41 | The Ubiquitin E1 Inhibitor, PYR-41 controls the biological activity of Ubiquitin E1. This small molecule/inhibitor is primarily used for Protease Inhibitors applications. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin from bovine erythrocytes | BioUltra, ?98% (SDS-PAGE), essentially salt-free, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin Isopeptidase Inhibitor I, G5 - CAS 108477-18-5 | The Ubiquitin Isopeptidase Inhibitor I, G5, also referenced under CAS 108477-18-5, controls the biological activity of Ubiquitin Isopeptidase. This small molecule/inhibitor is primarily used for Protease Inhibitors applications. Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-Specific Protease 10 human | recombinant, expressed in Sf9 cells, ?56% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-Specific Protease 14 human | recombinant, expressed in Sf9 cells, ?75% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-Specific Protease 5 human | recombinant, expressed in Sf9 cells, ?51% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Ubiquitin-Specific Protease 8 human | recombinant, expressed in Sf9 cells, ?70% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| ubiquitinyl hydrolase 1 | Links to polypeptides smaller than 60 residues are hydrolysed more readily than those to larger polypeptides. Isoforms exist with quantitatively different specificities, amongst the best known being UCH-L1 and UCH-L3, which are major proteins of the brain of mammals. Inhibited by ubiquitin aldehyde (in which Gly76 is replaced by aminoacetaldehyde). Ubiquitinyl hydrolase 1 is the type example of peptidase family C12, with a similar protein fold to papain and catalytic amino acids Cys, His and Asp. There is a separate family (C19) of enzymes that also hydrolyse ubiquitinyl bonds, and it is thought that all the ubiquitinyl hydrolases are also ubiquitin thiolesterases (EC 3.1.2.15). Group: Enzymes. Synonyms: ubiquitin C-terminal hydrolase; yeast ubiquitin hydrolase. Enzyme Commission Number: EC 3.4.19.12. CAS No. 86480-67-3, 189642-63-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4084; ubiquitinyl hydrolase 1; EC 3.4.19.12; 86480-67-3, 189642-63-5; ubiquitin C-terminal hydrolase; yeast ubiquitin hydrolase. Cat No: EXWM-4084. | |
| Ublituximab | Ublituximab (LFB-R603; TG-1101; TGTX-1101) is a next-generation, type 1 chimeric monoclonal antibody targeting a unique epitope on the CD20 antigen. Ublituximab has anticancer effects [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: LFB-R603; TG-1101; TGTX-1101. CAS No. 1174014-05-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99538. | |
| UBP1112 | UBP1112. Group: Biochemicals. Grades: Purified. CAS No. 339526-74-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UBP 282 | UBP 282. Group: Biochemicals. Grades: Purified. CAS No. 544697-47-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UBP 296 | UBP 296. Group: Biochemicals. Grades: Purified. CAS No. 745055-86-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UBP 301 | UBP 301. Group: Biochemicals. Grades: Purified. CAS No. 569371-10-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UBP302 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UBP 302 | UBP 302. Group: Biochemicals. Grades: Purified. CAS No. 745055-91-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UBP 310 | UBP 310. Group: Biochemicals. Grades: Purified. CAS No. 902464-46-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UBP310 (GluK1/GluK3 Antagonist, UBP310, (S)-1-(2-Amino-2-carboxyethyl)-3-(2-carboxy-thiophene-3-yl-methyl)-5-methylpyrimidine-2,4-dione, UBP-310, UBP 310) | A potent antagonist highly selective for GluK1 (Kb = 10nM), GluK3 (IC50 = 23nM), and GluK1/K5 (Kb = 8nM) subtype kainate receptors. Does not interact with GluK2 and GluK2/K5 receptors. Low affinity to AMPA receptors (Kd = 83uM). Does not interact with mGluR1 ornMDA receptors at concentration less than 10uM. Often used in studying neuronal excitability and synaptic plasticity. Group: Biochemicals. Grades: Highly Purified. CAS No. 902464-46-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| UBP608 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UBP714 | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Ubrogepant | Ubrogepant (MK-1602) is an orally active and selective antagonist of calcitonin gene-related peptide receptor ( CGRP ). Ubrogepant has high affinity for CGRP receptors in human and rhesus monkeys, and can effectively block the cAMP response stimulated by α-CGRP. Ubrogepant can be used in the study of acute migraine [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-1602. CAS No. 1374248-77-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12366. | |
| UBX1325 | UBX1325 is an Bcl-xL inhibitor that promotes apoptosis in senescent cells. UBX1325 is a potent anti-aging agent that can be used in studies of age-related eye diseases such as diabetic macular oedema (DME), age-related macular degeneration (AMD) and diabetic retinopathy (DR)[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2271269-01-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-150069. | |
| UBX domain-containing protein 11 (447-460) | UBX domain-containing protein 11 (447-460) is a peptide derived from UBX domain-containing protein 11. UBX domain-containing protein 11 is involved in the reorganization of actin cytoskeleton mediated by RND1, RND2 AND RND3. It promotes RHOA activation mediated by GNA12 and GNA13. Synonyms: Colorectal tumor-associated antigen COA-1 (447-460); UBX domain-containing protein 5 (447-460). | |
| UC 112 | UC 112. Group: Biochemicals. Grades: Purified. CAS No. 383392-66-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UC2288 | UC2288 is a potent and orally active p21 attenuator (relatively selective activity for p21), which is synthesized based Sorafenib (HY-10201). UC2288 potently inhibits cancer cell growth by inducing apoptosis. UC2288 has no inhibition of VEGFR2 and Raf kinases even at 10 ?M[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1394011-91-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-112780. | |
| UCA 1064-A | UCA 1064-A is an antitumor antibiotic isolated from Wallemia sebi, which inhibits HeLa S3 cells with IC50 of 12.7 μmol/L, suppresses saccharomyces cerevisiae and gram-positive bacteria with MIC of 0.05 and 40 μg/mL, respectively. Molecular formula: C28H45NO. Mole weight: 411.66. | |
| UCA 1064-B | UCA 1064-B is an antitumor antibiotic isolated from Wallemia sebi, which inhibits HeLa S3 cells with IC50 of 14.8 μmol/L, suppresses saccharomyces cerevisiae and gram-positive bacteria with MIC of 0.39 and 40 μg/mL, respectively. Molecular formula: C28H47NO. Mole weight: 413.68. | |
| Ucar Solution Vinyl Resin 9003-22-9 | Ucar Solution Vinyl Resin - Surface Coatings. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| UCB 35625 | UCB 35625. Group: Biochemicals. Grades: Purified. Pack Sizes: 1mg, 10mg. US Biological Life Sciences. | Worldwide |
| UCB-6876 | UCB-6876 is a TNF? inhibitor. UCB-6876 can specifically bind to the asymmetric crystalline form of the TNF-? trimer, with a KD of 22 ?M[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 637324-45-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156454. | |
| UCB-9260 | UCB-9260, an orally active compound, inhibits TNF signaling by stabilising an asymmetric form of the trimer. UCB-9260 is selective for TNF over other superfamily members, and binds TNF with a similar Kd of 13?nM[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1515888-53-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-133122. | |
| UCD38B hydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UCE1022 | UCE1022 is a cytotoxin with topoisomerase I mediated DNA cleavage activity. Synonyms: UCE-1022; UCE 1022. CAS No. 158243-10-8. Molecular formula: C18H10O10S. Mole weight: 418.3. | |
| UCE 6 | UCE 6 is an antitumor metabolite with topoisomerase I mediated DNA cleavage activity. Synonyms: UCE-6; UCE6. CAS No. 150829-94-0. Molecular formula: C24H20O8. Mole weight: 436.4. | |
| Ucenprubart | Ucenprubart is an anti- CD200R1 human IgG4κ monoclonal antibody [1]. Recommend Isotype Controls: Human IgG4 kappa, Isotype Control (HY-P99003). Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2414559-57-0. Pack Sizes: 1 mg. Product ID: HY-P990770. | |
| Ucf-101 | Ucf-101 is a selective and competitive inhibitor of pro-apoptotic protease Omi/HtrA2 , with an IC 50 of 9.5 μM for His-Omi. Ucf-101 exhibits very little activity against various other serine proteases (IC 50 >200 μM). Ucf-101 has a natural red fluorescence at 543 nm that is used to monitor its ability to enter mammalian cells. Ucf-101 has a significant cardioprotective effect against MI/R injury and also has certain neuroprotective effect [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 313649-08-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-125959. | |
| UCF-101 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UCF116-A | UCF116-A is a FTase inhibitor produced by Steptomyces sp. Molecular formula: C37H48N2O8. Mole weight: 648.78. | |
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